FDAJuly 12, 2018device
OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right, REF ZBH-PSNCREF311-R.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
What to do
FDA enforcement status: Terminated
Brands named
orthosensor
UPCs
00816818021447
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAOrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Right, REF ZBH-PSNCRGH712-R.2018-07-12
- FDAOrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left, REF ZBH-PSNCREF311-L.2018-07-12
- FDAOrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Left, REF ZBH-PSNCRGH712-L.2018-07-12
- FDAOrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Left, REF ZBH-PSNCRCD39-L.2018-07-12
- FDAOrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right, REF ZBH-PSNCRCD39-R.2018-07-12
- FDAVerasense Knee System, Model SYK-TRCR 02. Intelligent disposable tibial insert that measures dynamic loads during orthopedic knee surgery.2014-12-05
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